Abstract
WE have provided evidence that: (a) lethality of mice to crude Bothrops venom varies according the isogenic strain (A/J > C57B1/6 > A/Sn > BALB/c > C3H/ HePas > DBA/2 > C3H/He); (b)BALB/c mice (LD50=100.0μg) were injected i.p. with 50 μg of venom produced IL-6, IL-10, INF-γ, TNF-α and NO in the serum. In vitro the cells from the mice injected and challenged with the venom only released IL-10 while peritoneal macrophages released IL-10, INF- γ and less amounts of IL-6; (c) establishment of local inflammation and necrosis induced by the venom, coincides with the peaks of TNF-α, IFN-γ and NO and the damage was neutralized when the venom was incubated with a monoclonal antibody against a 60 kDa haemorrhagic factor. These results suggest that susceptibility to Bothrops atrox venom is genetically dependent but MHC independent; that IL-6, IL-10, TNF-α, IFN-γ and NO can be involved in the mediation of tissue damage; and that the major venom component inducers of the lesions are haemorrhagins.
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Barros, S. F., Friedlanskaia, I., Petricevich, V. L., & Kipnis, T. L. (1998). Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom. Mediators of Inflammation, 7(5), 339–346. https://doi.org/10.1080/09629359890866
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